Delivering sufficient water to the evaporation surface/interface is one of the most widely adopted strategies to overcome salt accumulation in solar‐driven interfacial desalination. However, water transport and heat conduction loss are positively correlated, resulting in the trade‐off between thermal localization and salt resistance. Herein, a 3D hydrogel evaporator with vertical radiant vessels is prepared to surmount the long‐standing trade‐off, thereby achieving high‐rate and stable solar desalination of high‐salinity. Experiments and numerical simulations reveal that the unique hierarchical structure, which consists of a large vertical vessel channel, radiant vessels, and porous vessel walls, facilitates strong self‐salt‐discharge and low longitudinal thermal conductivity. With the structure employed, a groundbreaking comprehensive performance, under one sun illumination, of evaporation rate as high as 3.53 kg m−2 h−1, salinity of 20 wt%, and a continuous 8 h evaporation is achieved, which thought to be the best reported result from a salt‐free system. This work showcases the preparation method of a novel hierarchical microstructure, and also provides pivotal insights into the design of next‐generation solar evaporators of high‐efficiency and salt tolerance.

Coping with the shortage of fresh water and electricity in off-grid and resource-constrained areas through sustainable strategies has become the most urgent challenge facing the development of human society. Herein, we propose a low-cost and sustainable way of repurposing discarded pomelo peel by converting it into 3D porous carbon foam (i.e., carbonized pomelo peel, referred to as CPP) with multichannel waterways for synergetic coupling of solar-driven interfacial evaporation (SDIE) and low-grade heat-to-electricity generation. The superhydrophilic 3D porous CPP with multichannel waterways utilizes its powerful water supply capability to avoid salt accumulation during continuous seawater desalination. By cautiously weighing the water transport and thermal management of CPP-based evaporators, CPP with three-channel waterways (CPP3) can achieve efficient solar-driven evaporation (the evaporation rate of 1.37 kg m −2 h −1 , one sun) on the premise of salt resistance through its superior light absorption and ultrafast solar-thermal response. Besides, a collaborative device integrating CPP3 and a commercial thermoelectric (TE) generator is designed for synchronous generation of solar steam and thermoelectricity, which can simultaneously achieve an evaporation rate of 1.39 kg m −2 h −1 and a power output of 0.5 W m −2 under one sun illumination. Such a cost-effective and easy-to-manufacture strategy can provide potential opportunities for satisfying the demand for fresh water and electricity in resource-constrained areas.

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The development of an efficient pH‐universal hydrogen evolution reaction (HER) electrocatalyst is essential for practical hydrogen production. Here, an efficient and stable pH‐universal HER electrocatalyst composed of the strongly coupled 2D NiCo2S4 and 2D ReS2 nanosheets (NiCo2S4/ReS2) is demonstrated. The NiCo2S4/ReS2 2D–2D nanocomposite is directly grown on the surface of the carbon cloth substrate, which exhibits excellent HER performance with overpotentials of 85 and 126 mV at a current density of 10 mA cm−2 and Tafel slopes of 78.3 and 67.8 mV dec−1 under both alkaline and acidic conditions, respectively. Theoretical and experimental characterizations reveal that the chemical coupling between NiCo2S4 and ReS2 layers induces electron transfer from Ni and Co to interfacial Re‐neighbored S atoms, enabling beneficial H atom adsorption and desorption for both acidic and alkaline HER. Simultaneously, an electron transfer‐induced spin‐crossover generates high‐spin interfacial Ni and Co atoms that promote water dissociation kinetics at the NiCo2S4/ReS2 interface, which is the origin of the superior alkaline HER activity. NiCo2S4/ReS2 also shows decent catalytic activity and long‐term durability for oxygen evolution reaction, and finally bifunctionality for overall water splitting. This study suggests a rational strategy to enhance water dissociation kinetics by inducing spin‐crossover via electron transfer.

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There is an increasing demand for high-density memories with high stability for supercomputers in this big data era.